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1-Bromo-4-tert-butylbenzene

  • Product Name: 1-Bromo-4-tert-butylbenzene
  • CasNo: 3972-65-4
  • Purity:
  • Appearance: clear colorless to slightly yellow liquid

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CasNo: 3972-65-4

Molecular Formula: C10H13Br

Appearance: clear colorless to slightly yellow liquid

Quality Factory Sells Top Purity 99% 1-Bromo-4-tert-butylbenzene 3972-65-4 with Safe Delivery

  • Molecular Formula:C10H13Br
  • Molecular Weight:213.117
  • Appearance/Colour:clear colorless to slightly yellow liquid 
  • Vapor Pressure:0.0916mmHg at 25°C 
  • Melting Point:13-16 °C(lit.) 
  • Refractive Index:n20/D 1.533(lit.)  
  • Boiling Point:232 °C at 760 mmHg 
  • Flash Point:97.2 °C 
  • PSA:0.00000 
  • Density:1.236 g/cm3 
  • LogP:3.74660 

3972-65-4 Relevant articles

Photochemical Sandmeyer-type Halogenation of Arenediazonium Salts

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supporting information, (2022/01/19)

Trihalide salts were found to efficientl...

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Methyl groups are ubiquitous in biologic...

Visible-Light-Photosensitized Aryl and Alkyl Decarboxylative Functionalization Reactions

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, p. 10514 - 10520 (2019/07/12)

Despite significant progress in aliphati...

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, p. 930 - 938 (2018/01/28)

Regioselective halogenation of arenes an...

3972-65-4 Process route

(P(o-tol)<SUB>3</SUB>)<SUB>2</SUB>Pd<SUB>2</SUB>(C<SUB>6</SUB>H<SUB>4</SUB><SUP>t</SUP>Bu-4)<SUB>2</SUB>Br<SUB>2</SUB>
176780-03-3,164927-39-3

(P(o-tol)3)2Pd2(C6H4tBu-4)2Br2

tri-tert-butyl phosphine
13716-12-6

tri-tert-butyl phosphine

bis(tri-t-butylphosphine)palladium<sup>(0)</sup>
53199-31-8

bis(tri-t-butylphosphine)palladium(0)

1-bromo-4-tert-butylbenzene
3972-65-4

1-bromo-4-tert-butylbenzene

Conditions
Conditions Yield
In benzene-d6; byproducts: P(o-tol)3, biaryl, arene; in C6D6 soln. at 70°C; K(eq) = 3.3(6)E-4;
75%
tert-butylbenzene
253185-03-4,253185-04-5

tert-butylbenzene

1-bromo-4-tert-butylbenzene
3972-65-4

1-bromo-4-tert-butylbenzene

Conditions
Conditions Yield
With bromine; iodine; at 0 ℃;
100%
With carbon dioxide; bromine; at 40 ℃; for 2h; under 187519 Torr; Supercritical conditions; Green chemistry;
100%
With benzyltrimethylazanium tribroman-2-uide; zinc(II) chloride; In acetic acid; at 70 ℃; for 2h;
95%
With bromine fluoride; In ethanol; chloroform; at -78 ℃; for 0.0833333h;
89%
With thallium (III) oxide; trifluoroacetic acid; potassium bromide; at 20 ℃; for 25h;
86%
With Li2MnO3; bromine; oxygen; at 80 ℃; for 3h; under 760.051 Torr; Photolysis;
86%
With bromine; iron; In tetrachloromethane; at 0 ℃; for 1h;
84%
With bromine; In dichloromethane; at 0 ℃; Inert atmosphere;
80%
With bromine; iron; In dichloromethane; at 5 - 20 ℃; for 24h;
71%
With styrene-4-vinyl(N-alkylpyridinium bromide); In water; acetic acid; at 85 ℃; for 5h;
59%
With bromine; Sonnenlicht;
With bromine; iron;
With iodine; durch Bromierung;
With iron; durch Bromierung;
With bromine; iron;
With bromine;
With bromine; iodine; iron;
With bromine; acetic anhydride; zinc(II) chloride; In acetic acid;
With bromine; iron;
With pyridine; bromine;
With sodium metabisulfite; bromine; Irradiation;
With bromine fluoride; ethanol; Yield given. Multistep reaction; 1.) CFCl3, -75 deg C; 2.) CHCl3, -75 deg C, 5-15 min;
With bromine; ZnBr2 on silica (100 Angstroem); In hexane; at 25 ℃; for 0.0333333h; Yield given;
With zeolite NaY; bromine; In dichloromethane; at 20 ℃; for 5h;
97 % Chromat.
Multi-step reaction with 2 steps
1: AlCl3 / 45 °C
2: iron-turnings; tetrachloromethane; bromine
With tetrachloromethane; aluminium trichloride; bromine; iron;
With N-Bromosuccinimide; at 20 ℃; for 16h; regioselective reaction;

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